Noga Therapeutics

Product pipeline

Parkinson’s disease

Parkinson’s disease primarily affects movement and causes symptoms such as tremors, stiffness, and impaired balance and coordination. The disease is caused by the degeneration of dopamine-producing neurons. The exact cause of this neurodegeneration is not fully understood, but a combination of genetic and environmental factors is thought to play a role.

Current solutions are limited

The standard of care for Parkinson’s disease is a dopamine replacement drug invented in the 1960s named Levodopa. This treatment has serious side-effects and often requires the use of devices that continuously deliver Levodopa. These devices have a significant toll on patients’ quality of life and are associated with various complications.


Patients by 2040

Up to 10%

of people with Parkinson’s are diagnosed before age 50


Total economic burden in the US

Our solution - DopaGeneTM

Noga is developing DopaGene™, a novel gene-therapy-based solution for direct dopamine production in the brain.
In a single, non-invasive procedure, Parkinson’s disease patient’s own blood stem cells are engineered with DopaGene™ and then re-infused into the bloodstream.
Macrophages that develop from the engineered stem cells migrate to the brain, where they settle and produce safe and effective levels of dopamine for years to come.
Local dopamine production eliminates the harsh side-effects of dopamine replacement-based products.

X-linked Agammaglobulinemia (XLA)

XLA is a rare genetic primary immunodeficiency caused by a mutation in a gene named BTK. This genetic mutation leads to a failure of B-cell maturation and disrupts the ability of the patients to produce antibodies. Without treatment, XLA patients would suffer from recurrent infections that will eventually lead to death.

Current solutions are limited

Current therapy consists of life-long administration of pooled human antibody replacement therapy and targeted antimicrobial agents. This treatment is insufficient, and even with treatment, XLA patients have a reduced lifespan and suffer frequent and serious health complications.

Our solution - BTK-001

BTK-001 is a lentiviral vector-based gene therapy designed to re-engineer XLA patient’s own stem cells by delivering the BTK gene directly to stem cells. Upon stem-cell reprograming, patients regain the ability to develop B-cells and produce antibodies, essentially being cured from the disease after a single treatment.

US Patent status: Granted- #US11464872

BTK-001 treatment restores the capacity of mice with XLA to produce antibodies

BTK-001 path to the clinic

Proof of concept in XLA mouse model

A US patent was granted

Positive feedback from the FDA

First-in-human at Schneider Children’s Medical Center

Sefi Golan


Sefi is a 22-year entrepreneur who founded a Nasdaq-listed company. He has a proven track record of assembling exceptional teams and building technology ahead of its time.
Sefi founded HUB Cyber Security, which reached a peak market capitalization of $350 million. He also advised Bancor, which raised $153 million and reached a peak market capitalization of $800 million.
Currently Sefi is heading the investment team in a privately owned family office.
Sefi holds a B.Sc. in Business Administration and Economics from the University of Tel Aviv.

Adam Brian

Head of Personalized Medicine at Lonza

Mr.  Adam Brian heads Lonza Personalized Medicine, which focuses on developing and bringing to market tools that enable research and development, scale out, and commercialization of patient scale cell therapies, with an emphasis on decentralized and point of care manufacturing. Mr. Brian  is a results-oriented leader with extensive experience in the life science and medical device industries. Proven track record of increasing revenue, improving operations, and building and leading high-performing teams. 

Dr. Eytan Abraham

VP, Business Head of Cell, Gene and Nucleic Acids Franchises, Resilience

 Dr. Eytan Abraham heads Resilience cell, gene and nucleic acids Franchises. Dr. Abraham holds a Ph.D. in developmental and molecular biology from the University of Maryland Biotechnology Institute, and a post-doctorate in cell-therapy and tissue engineering from the Harvard-MIT Biomedical Engineering Center and Harvard Medical School. Dr. Abraham is an experienced scientist and business leader with expertise in basic and applied biological and cell therapy R&D as well as in management, technology, and commercialization.

Anat Naschitz

CEO and Co-Founder - 9xchange

Anat Naschitz is a lifescience investor and entrepreneur, with 27 years of experience across biotech, pharma, digital health and medical devices. 

Anat co-founded and co-led OrbiMed Israel, an Israel focused VC fund and part of the leading, $20bn global healthcare investment firm, and was previously with Apax, the €60bn private equity firm, where she started her investment career. Previously Anat was an Associate Partner with McKinsey in London, where she advised the world’s preeminent pharmaceutical companies on strategy, acquisitions and spinouts.

Throughout her career Anat has founded companies and nurtured them through success. Examples include 89bio (Nasdaq:ETNB), developing a likely best in class therapeutic for NASH, which she co-founded and spun out of Teva, taking it public on Nasdaq 18 months post creation, currently trading at $1bn; Sobi, which evolved out of a Pharmacia spinout and currently trading at $7.4bn; and many others. 

Currently, Anat is co-founder and CEO of 9xchange, a biopharma marketplace, creating transparency and enabling the ecosystem to monetize pipelines and discover assets whose availability was unknown, through a seamless, initially anonymous, AI-driven process. 

Anat earned her MBA at Insead in France and her LLB at Tel Aviv University.

Dr. Yael Weiss

CEO - Mahzi Therapeutics

Dr. Yeal Weiss is currently CEO of Mahzi Therapeutics, a company focused on the development of therapies for ultra-rare genetic neurodevelopmental disorders. Dr. Weiss completed her MD at Hadassah Medical School at the Hebrew University in Jerusalem and her PhD at the Weizmann Institute of Science in Rehovot, Israel. She has over 20 years of industry experience in medical/clinical and business development roles at Genzyme, Merck and Ultragenyx. Dr. Weiss is a member of the NIH driven Bespoke Gene Therapy (BCTG) consortium, ASGCT translational committee, N=1 collaborative and is a 2022 Termeer Fellow. Board member/advisor to ADNP and FOXG1 foundations.

Noam Baumatz


Noam is a physician with 20 years of experience in the field of complementary medicine (Brighton University). He formerly headed the Chinese Medicine Unit at Sheba Hospital. Noam is the founder and CEO of the Association for Noga (Her Way), which develops advanced therapies for ultra-rare diseases.

Dr. Liron Elkouby

Scientific Advisor

Liron brings many years of experience in cell- and gene-therapy translation. Prior to joining NOGA Therapeutics, Liron headed the discovery and the early-phase development of oncology at Enlivex Therapeutics. Prior to that, Liron led the hemophilia A program (currently in phase III) at Spark Therapeutics, USA. Liron holds a PhD from and conducted postdoctoral research at the Technion.

Dr. Noam Diamant


Noam previously co-founded Emendo Biotherapeutics, a leading CRISPR company that was acquired by Anges, Japan, in 2020, for $295M. As an expert on intellectual property strategies at Ingenium IP, Noam advised dozens of biomed companies on building their IP-business strategy. Noam holds a PhD from the Weizmann Institute of Science in the field of DNA damage repair.